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PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly
由 Mzoughi, S., Di Tullio, F., Low, D.H.P., Motofeanu, C.-M., Ong, S.L.M., Wollmann, H., Wun, C.M., Kruszka, P., Muenke, M., Hildebrandt, F., Dunn, N.R., Messerschmidt, D.M., Guccione, E.
出版 2021
獲取全文出版 2021
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